Perin Health System (PHD80060-2)

FDA 510(k) K252984 · Perin Health Devices, LLC

Substantially Equivalent

510(k) numberK252984

Submission

Device name
Perin Health System (PHD80060-2)
Applicant
Perin Health Devices, LLC
Oklahoma City, OK, US
Received
September 18, 2025
Decision date
January 22, 2026
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DRG – Transmitters And Receivers, Physiological Signal, Radiofrequency
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2910
Specialty
Cardiovascular

Other 510(k)s with product code DRG

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K261569UbiqVue™ 2AYe Cardiac System (UX2253)DRG · Traditional Lifesignals, Inc.07/09/2026SE
K252440EasyTeleMed (2.0.2)DRG · Traditional Ingeniars S.R.L.10/02/2025SE
K250259TeleRehab Aermos Cardiopulmonary RehabilitationDRG · Traditional The ScottCare Corporation06/04/2025SE
K243837iBSMDRG · Traditional Iorbit Digital Technologies Private Limited05/16/2025SE
K242018UbiqVue™ 2A Multi-parameter System (UX2550)DRG · Traditional Lifesignals, Inc.11/12/2024SE
K241101BioButton SystemDRG · Traditional Biointellisense, Inc.09/26/2024SE
K240251ANNE ChestDRG · Traditional Sibel Health, Inc.06/03/2024SE
K223711ANNE OneDRG · Traditional Sibel Health, Inc.08/10/2023SE
K220526HD+12, HD+15DRG · Traditional Cardioline S.P.A05/15/2023SE
K223073AlioDRG · Traditional Alio, Inc.03/17/2023SE

Questions and answers

When was Perin Health System (PHD80060-2) cleared by the FDA?

Perin Health System (PHD80060-2) (K252984) received a 510(k) decision of Substantially Equivalent on January 22, 2026, 126 days after the submission was received.

What is the product code of K252984?

The FDA product code is DRG – Transmitters And Receivers, Physiological Signal, Radiofrequency, a Class II (moderate risk) device regulated under 21 CFR 870.2910.